A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856933



Internal ID22631868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:116567676..116570083hg38UCSC Ensembl
chr12:117005481..117007888hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg382408
hg192408
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467430
Samples
Known GenesMAP1LC3B2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856933
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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